US3259581A - Liquid developer for electrostatic images - Google Patents
Liquid developer for electrostatic images Download PDFInfo
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- US3259581A US3259581A US237294A US23729462A US3259581A US 3259581 A US3259581 A US 3259581A US 237294 A US237294 A US 237294A US 23729462 A US23729462 A US 23729462A US 3259581 A US3259581 A US 3259581A
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- carbon black
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- polarity
- zinc
- cobalt
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- 239000007788 liquid Substances 0.000 title claims description 30
- 239000006229 carbon black Substances 0.000 claims description 37
- 239000002245 particle Substances 0.000 claims description 35
- 239000000344 soap Substances 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 239000003381 stabilizer Substances 0.000 claims description 13
- 239000000725 suspension Substances 0.000 claims description 12
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 9
- 150000002739 metals Chemical class 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- 239000011575 calcium Substances 0.000 claims description 7
- 239000010941 cobalt Substances 0.000 claims description 7
- 229910017052 cobalt Inorganic materials 0.000 claims description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 7
- 239000011133 lead Substances 0.000 claims description 7
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 5
- 230000005686 electrostatic field Effects 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 claims description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims 4
- 229940105289 carbon black Drugs 0.000 description 33
- 235000019241 carbon black Nutrition 0.000 description 33
- 239000000049 pigment Substances 0.000 description 19
- 239000011347 resin Substances 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000002966 varnish Substances 0.000 description 16
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 12
- 239000005012 oleoresinous Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 239000004215 Carbon black (E152) Substances 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000011787 zinc oxide Substances 0.000 description 6
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 5
- 235000021388 linseed oil Nutrition 0.000 description 5
- 239000000944 linseed oil Substances 0.000 description 5
- 238000009736 wetting Methods 0.000 description 5
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 4
- 230000011514 reflex Effects 0.000 description 4
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- 125000005609 naphthenate group Chemical group 0.000 description 3
- 125000005474 octanoate group Chemical group 0.000 description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 3
- 239000006237 Intermediate SAF Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- DWPDSISGRAWLLV-JHZYRPMRSA-L calcium;(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Ca+2].C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O.C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O DWPDSISGRAWLLV-JHZYRPMRSA-L 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 2
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- NKFIBMOQAPEKNZ-UHFFFAOYSA-N 5-amino-1h-indole-2-carboxylic acid Chemical compound NC1=CC=C2NC(C(O)=O)=CC2=C1 NKFIBMOQAPEKNZ-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- IIGAELMXVLEZPM-GRVYQHKQSA-L cobalt(2+);(9z,12z)-octadeca-9,12-dienoate Chemical compound [Co+2].CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O.CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O IIGAELMXVLEZPM-GRVYQHKQSA-L 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/12—Developers with toner particles in liquid developer mixtures
- G03G9/135—Developers with toner particles in liquid developer mixtures characterised by stabiliser or charge-controlling agents
- G03G9/1355—Ionic, organic compounds
Definitions
- This invention relates to method and means for producing black developers, or toners as they are often called, suitable for dispersion in a liquid of relatively high electrical resistivity such as used in the known art of electrophotography as the liquid developer vehicle.
- this invention relates to the method and means of making the suspended toner particles capable of assuming a positive electrostatic charge in the presence of a latent image formed by a negative electrostatic charge.
- This particular embodiment of the present invention ensures that such suspended toner particles can become attracted only by negatively charged image areas and that consequently no deposition can take place on non-image areas or on areas free of negative charge.
- a further feature of this invention is that developers prepared in a manner as herein described will remain stable in suspension in respect of polarity characteristics for a period of time which is adequate for all practical purposes.
- electrophotographic images can be produced on surfaces containing photoconductive matter, and liquid developer formulations capable of producing images in various colours are also known. If the photoconductor used in the process is zinc oxide, which substance is not capable of supporting a positive electrostatic charge, it is then necessary for the developer particlessuspended in a liquid carrier medium to assume posi tive polarity in respect to the latent electrostatic image formed on the zinc oxide surface, because such latent image on a zinc oxide surface can be formed essentially by a negative electrostatic charge only.
- control agents in the form of a thin coating around the particulate pigment matter in suspension and it is said that this can be attained if the pigment is milled or ground with such resin or oil to form a paste which is then dispersed in the carrier liquid. It has been said that such control agents act by imparting their own characteristics of polarity to the enveloped pigment particle.
- Polarity control agents can be eifective only if they remain in the form of a thin adsorbed layer around each pigment particle in suspension. If the control agent is of oleoresinous nature, then this requirement can be achieved only if such oleoresinous matter is insoluble or only partly soluble in the particular carrier fluid for which it is intended to be used and if each pigment particle is uniformly wetted by the control agent. It the wetting of the pigment is done by appropriate mechanical means, such as milling or grinding, the uniformity of wetting will depend on the adsorption characteristics of each pigment particle, which, in case of carbon black pigments, is known to vary due to the presence of gaseous or other matter adsorbed onto the particles.
- the non-uniform wetting of carbon black particles by an oleoresinous control agent causes such oleoresinous matter to dissociate from certain particles more readily than from other particles so that effective polarity control by this method becomes impractical.
- an improved ,ticles suspended in the said carrier liquid as a toner said carbon black particles having previously been wetted by coating with an oil or oleoresinous varnish as a dispensing medium, and a metallic soap in a hydocarbon solvent in contact with the said coated particles as a polarity stabiliser.
- the metallic soaps can be such compounds. as oleates, linoleates, octoates, tallates, resinates, palmitates, stearates and naphthenates of such metals as lead, manganese, cobalt, calcium, aluminum, zinc and the like, and the solutions of such metallic soaps in a hydrocarbon solvent can be introduced either by milling together with the carbon black pigment and oil or oleoresinous varnish or they can be introduced directly into the carrier liquid prior, after or during the dispersion of the carbon black pigment which has been milled or ground with an oilor an oleoresinous varnish.
- the metallic soaps adsorb in suspension preferentially onto the carbon black particles and surprisingly render such particles capable of assuming a positive electrostatic charge in presence of a negative field or of a negative electrostatic latent image.
- the resins and oleoresinous varnishes used in accordance with this invention are present essentially as wetting agents for breaking up particle agglomerates during milling and for the purpose of aiding dispersion.
- the photoconductive material can be a relatively conducting backing or support such as paper or metal sheet or film upon which is deposited a coating comprising a particulate photoconductor capable of supporting a negative electrostatic charge such as zinc oxide or the like in a resin binder and such resin binder being capable of attaining a degree of hardness sufiicient to prevent the resin from being attacked or softened during contact with the carrier fluid.
- a coating comprising a particulate photoconductor capable of supporting a negative electrostatic charge such as zinc oxide or the like in a resin binder and such resin binder being capable of attaining a degree of hardness sufiicient to prevent the resin from being attacked or softened during contact with the carrier fluid.
- ingredients can be milled together, diluted if required, and then deposited on a relatively conducting support by any known coating method.
- An alternative to this formulation is the following:
- the ingredients can be milled together, diluted if required, and. deposited onto a support by any known coating method.
- the photoconductive material thus prepared and sufiiciently hardened can be now sensitized by subjecting it to a corona discharge from a series of wires or points held at a relatively high direct current potential above the base plate upon which the material is placed, the polarity being such as to impart a negative electrostatic blanket charge to the photoconductive layer.
- the material is then subjected to a light pattern whereby non-image areas are rendered conductive and permit the charge to dissipate into the relatively conducting support or backing whereas under the shielded image areas a latent image consisting of the remaining negative charge is formed.
- the developing step can be performed by immersing the photoconductive material in a vessel containing the liquid developer, or by mechanical means such as wet roller and squeegee, or cascading and the like.
- the liquid developer can be made up by dispersing any of the toners described in the following examples in the specified liquids in proportions ranging from 1 part toner to 100 or 200 parts of liquid by weight, or less or more, depending on the developing process preferred.
- toner formulations illustrate the use of metallic soaps in accordance with this invention and it will be realised that this invention is not restricted by the cited combinations of metallic soaps and varnishes and that one skilled in the art of making electrophotographic developers can adjust and select metallic soaps to suit particular varnishes, particular grades of carbon black and particular carrier liquids.
- Aluminum stearate (2% solution in Solvesso 100), (polarity stabiliser) 25 These components are hot blended, the heating being continued for such time as is necessary to reduce the volume of the compound by one quarter, due to solvent evaporation, after which the toner is remilled.
- This toner is stable in respect of polarity in carrier liquids such as Shell X55, Freon 113, n-hexane, n-heptane and cyclohexane.
- EXAMPLE 2 In perchloroethylene and Solvesso 100 the stability of the toner from Example 1 may be found to be inadequate. For increasing the stability in respect to polarity in perchloroethylene and Solvesso 100, mix- Grams Toner from Example 1 10 6% cobalt octoate (in a hydrocarbon solvent) polarity stabiliser 1 EXAMPLE 3 Carbon black ISAF (pigment) 40 Reflex blue in varnish No.
- This toner is stable in respect to polarity in liquid carriers such as Shell X55, Freon 11, Freon 113, n-hexane, n-heptane and cyclohexane.
- EXAMPLE 4 Grams Carbon black SRF 40 Superbeckacite 2100 resin varnish in bodied linseed oil (20% resin) Q: 100 8.5% cobalt linoleate (in hydrocarbon solvent) polarity stabiliser 60 16% lead tallate (in hydrocarbon solvent) polarity stabiliser 10 Cold blend ingredients and mill.
- This toner is stable in respect to polarity in carrier liquids such as Shell X55, n-hexane, n-heptane, Freon 11, Freon 113, cyclohexane, Solvesso 100 and perchloroethylene.
- carrier liquids such as Shell X55, n-hexane, n-heptane, Freon 11, Freon 113, cyclohexane, Solvesso 100 and perchloroethylene.
- the polarity of this toner is stable in Freon 113.
- the polarity of this toner is stable in Shell X4 and n-hexane.
- the polarity of this toner is stable in Shell X55, Shell X4, n-hexane, n-heptane, Freon 11, Freon 113, and cyclohexane.
- Carbon black ISAF particle size 23 millimicrons, manufactured by Australian Carbon Black Pty. Ltd.
- Carbon black SRF particle size '80 millimicrons, manufactured by Australian Carbon Black Pty. Ltd.
- Carbon black Vanblack HAF manufactured by R. T.
- Dyal XOR 36 modified ether resin, manufactured by Sherwin-Williams Co.
- Pentacite P-423 pentaerythritol resin, manufactured by Reichhold Chemical.
- a liquid developer for electrostatic images consisting essentially of an electrically insulating carrier liquid of volume resistivity in excess of 1 0 ohm centimeter and a dielectric constant less than 3, particles of carbon black suspended in said carrier liquid as a toner, said carbon black particles having been previously wetted by grinding in an oil-containing dispersing medium, and a metallic soap in contact with said suspended particles of carbon black as a polarity stabilizer imparting positive polarity to such particles at least in the presence of a negative electrostatic field, said metallic soap being present in such quantity that the metal content of the soap is at least one percent by Weight of the carbon black particles in suspension, and said metallic soap being selected from the group consisting of the linoleates of the metals cobalt, manganese, lead and zinc, naphthenates and resinates of the metals calcium, cobalt, manganese, lead and zinc, octoates and oleates of the metals calcium and cobalt, palrnitate of the metal zinc and steanates of the metal
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Liquid Developers In Electrophotography (AREA)
- Developing Agents For Electrophotography (AREA)
Description
United States Patent 3 Claims. (or. 252-621) This invention relates to method and means for producing black developers, or toners as they are often called, suitable for dispersion in a liquid of relatively high electrical resistivity such as used in the known art of electrophotography as the liquid developer vehicle. In particular this invention relates to the method and means of making the suspended toner particles capable of assuming a positive electrostatic charge in the presence of a latent image formed by a negative electrostatic charge. This particular embodiment of the present invention ensures that such suspended toner particles can become attracted only by negatively charged image areas and that consequently no deposition can take place on non-image areas or on areas free of negative charge.
A further feature of this invention is that developers prepared in a manner as herein described will remain stable in suspension in respect of polarity characteristics for a period of time which is adequate for all practical purposes.
It is known that electrophotographic images can be produced on surfaces containing photoconductive matter, and liquid developer formulations capable of producing images in various colours are also known. If the photoconductor used in the process is zinc oxide, which substance is not capable of supporting a positive electrostatic charge, it is then necessary for the developer particlessuspended in a liquid carrier medium to assume posi tive polarity in respect to the latent electrostatic image formed on the zinc oxide surface, because such latent image on a zinc oxide surface can be formed essentially by a negative electrostatic charge only. With certain exceptions, most pigments when associated with a resin or oil and suspended in an insulating liquid such as the hydrocarbon solvent known under the trade name Shell X55, of the Shell Company, will assume positive polarity in respect to a latent image formed by a negative elec trostatic charge, so that such latent image can be renderd visible because the pigment particles in suspension will deposit by electrostatic attraction onto the image areas.
It has been proposed heretobefore to use certain resins or oils' termed as control agents to impart the desired positive polarity to certain pigments which normally would assume fully or partially negative polarity in respect to a negative electrostatic latent image when suspended in an insulating carrier liquid and would therefore deposit onto the non-image areas to a greater or lesser degree, orwould deposit both onto the image and non image areas.
It has been also proposed to introduce such control agents in the form of a thin coating around the particulate pigment matter in suspension and it is said that this can be attained if the pigment is milled or ground with such resin or oil to form a paste which is then dispersed in the carrier liquid. It has been said that such control agents act by imparting their own characteristics of polarity to the enveloped pigment particle.
It is known to those skilled in the art of paint and printers ink making that carbon black pigments are difiicult to wet by oils or oleoresinous varnishes, and that the wetting properties of carbon black are largely dependent on the type and quantity of the gaseous or other matter which is known to be present in the form of an adsorbed "ice layer around carbon black particles. Such variation in the adsorbed matter is thought to be also responsible for carbon black particles suspended in an insulating liquid such as Shell X55 in absence of any oil or resin to assume dual polarity in presence of a negative electrostatic field or of a negative electrostatic latent image, with the effect that such carbon black particles will deposit both onto image and non-image areas.
Polarity control agents can be eifective only if they remain in the form of a thin adsorbed layer around each pigment particle in suspension. If the control agent is of oleoresinous nature, then this requirement can be achieved only if such oleoresinous matter is insoluble or only partly soluble in the particular carrier fluid for which it is intended to be used and if each pigment particle is uniformly wetted by the control agent. It the wetting of the pigment is done by appropriate mechanical means, such as milling or grinding, the uniformity of wetting will depend on the adsorption characteristics of each pigment particle, which, in case of carbon black pigments, is known to vary due to the presence of gaseous or other matter adsorbed onto the particles.
When suspended in a carrier liquid, the non-uniform wetting of carbon black particles by an oleoresinous control agent causes such oleoresinous matter to dissociate from certain particles more readily than from other particles so that effective polarity control by this method becomes impractical.
As an alternative to oleoresinous control agents, it has been also proposed heretobefore to use carbon black pigments in co-suspension with certain other pigments onto which the carbonblack particles precipitatein the course of deposition caused by electrostatic attraction and since such other pigments assume a positivepolarity in presence of a negative electrostatic field, the carbon black particles are thus also caused to deposit onto the image areas only. The disadvantage of developers prepared in this.
matter is that their stability in suspension and shelf-life is limited.
In accordance with the present invention an improved ,ticles suspended in the said carrier liquid as a toner, said carbon black particles having previously been wetted by coating with an oil or oleoresinous varnish as a dispensing medium, and a metallic soap in a hydocarbon solvent in contact with the said coated particles as a polarity stabiliser.
The metallic soaps can be such compounds. as oleates, linoleates, octoates, tallates, resinates, palmitates, stearates and naphthenates of such metals as lead, manganese, cobalt, calcium, aluminum, zinc and the like, and the solutions of such metallic soaps in a hydrocarbon solvent can be introduced either by milling together with the carbon black pigment and oil or oleoresinous varnish or they can be introduced directly into the carrier liquid prior, after or during the dispersion of the carbon black pigment which has been milled or ground with an oilor an oleoresinous varnish.
Whichever method is used, the metallic soaps adsorb in suspension preferentially onto the carbon black particles and surprisingly render such particles capable of assuming a positive electrostatic charge in presence of a negative field or of a negative electrostatic latent image.
It will be readily realised that there is great advantage in using polarity stabilising substances which adsorb from solution or suspension and which exhibit particular preference for adsorbing onto carbon black because subsequent dissociation of such adsorbed substance is very unlikely and therefore stability of polar behaviour is ensured.
It was found that depending on the oleoresinous varnish, the grade of carbon black pigment and the carrier fluid, a combination of two or more metallic soaps may be more effective than one type of metallic soap only and in the following formulations it will also be found that the manner in which the soaps can be incorporated varies accordingly.
The resins and oleoresinous varnishes used in accordance with this invention are present essentially as wetting agents for breaking up particle agglomerates during milling and for the purpose of aiding dispersion.
The following is a detailed description of the method by which a black electrophotographic image can be produced using the embodiment of this invention:
The photoconductive material can be a relatively conducting backing or support such as paper or metal sheet or film upon which is deposited a coating comprising a particulate photoconductor capable of supporting a negative electrostatic charge such as zinc oxide or the like in a resin binder and such resin binder being capable of attaining a degree of hardness sufiicient to prevent the resin from being attacked or softened during contact with the carrier fluid. The following photoconductive coating can be used in the liquid developer process:
Grams Zinc oxide Durham special Z 900 Rhodene M8/50 600 Toluol 250 4% manganese naphthenate 2.5 3% cobalt naphthenate 2.5
The ingredients can be milled together, diluted if required, and then deposited on a relatively conducting support by any known coating method. An alternative to this formulation is the following:
Grams Zinc oxide Durham special Z 750 Dyal XOR 36 416 Toluol 200 lead naphthenate 8.5 4% manganese naphthenate 3.5 3% cobalt naphthenate 4.5
Here again, the ingredients can be milled together, diluted if required, and. deposited onto a support by any known coating method. The photoconductive material thus prepared and sufiiciently hardened can be now sensitized by subjecting it to a corona discharge from a series of wires or points held at a relatively high direct current potential above the base plate upon which the material is placed, the polarity being such as to impart a negative electrostatic blanket charge to the photoconductive layer. The material is then subjected to a light pattern whereby non-image areas are rendered conductive and permit the charge to dissipate into the relatively conducting support or backing whereas under the shielded image areas a latent image consisting of the remaining negative charge is formed.
This latent image can now be rendered visible by developing it in any one of the liquid developers hereafter described. The developing step can be performed by immersing the photoconductive material in a vessel containing the liquid developer, or by mechanical means such as wet roller and squeegee, or cascading and the like. The liquid developer can be made up by dispersing any of the toners described in the following examples in the specified liquids in proportions ranging from 1 part toner to 100 or 200 parts of liquid by weight, or less or more, depending on the developing process preferred.
The following examples of toner formulations illustrate the use of metallic soaps in accordance with this invention and it will be realised that this invention is not restricted by the cited combinations of metallic soaps and varnishes and that one skilled in the art of making electrophotographic developers can adjust and select metallic soaps to suit particular varnishes, particular grades of carbon black and particular carrier liquids.
Aluminum stearate (2% solution in Solvesso 100), (polarity stabiliser) 25 These components are hot blended, the heating being continued for such time as is necessary to reduce the volume of the compound by one quarter, due to solvent evaporation, after which the toner is remilled.
This toner is stable in respect of polarity in carrier liquids such as Shell X55, Freon 113, n-hexane, n-heptane and cyclohexane.
EXAMPLE 2 In perchloroethylene and Solvesso 100 the stability of the toner from Example 1 may be found to be inadequate. For increasing the stability in respect to polarity in perchloroethylene and Solvesso 100, mix- Grams Toner from Example 1 10 6% cobalt octoate (in a hydrocarbon solvent) polarity stabiliser 1 EXAMPLE 3 Carbon black ISAF (pigment) 40 Reflex blue in varnish No. 69884 (added toner) 4 Superbeckacite 2100 resin varnish in bodied linseed oil (20% resin) (wetting and dispersing agent) 100 15% lead naphthenate (in hydrocarbon solvent) polarity stabiliser 50 50% calcium resinate (solution in Solvesso 100) polarity stabiliser 200 Cold blend ingredients and mill.
This toner is stable in respect to polarity in liquid carriers such as Shell X55, Freon 11, Freon 113, n-hexane, n-heptane and cyclohexane.
EXAMPLE 4 Grams Carbon black SRF 40 Superbeckacite 2100 resin varnish in bodied linseed oil (20% resin) Q: 100 8.5% cobalt linoleate (in hydrocarbon solvent) polarity stabiliser 60 16% lead tallate (in hydrocarbon solvent) polarity stabiliser 10 Cold blend ingredients and mill.
This toner is stable in respect to polarity in carrier liquids such as Shell X55, n-hexane, n-heptane, Freon 11, Freon 113, cyclohexane, Solvesso 100 and perchloroethylene.
EXAMPLE 5 Grams Carbon black Sterling MT 30 Reflex blue in varnish No. 69884 3 Calcium resinate varnish in bodied linseed oil (25% resin) partial polarity stabiliser 3% calcium naphthenate (in hydrocarbon solvent) polarity stabiliser 30 Cold blend ingredients and mill.
The polarity of this toner is stable in Freon 113.
EXAMPLE 6 Grams Toner from Example 5 3O lead naphthenate (in hydrocarbon solvent) additional polarity stabiliser 1O Blend ingredients and mill.
The polarity of this toner is stable in Shell X4 and n-hexane.
EXAMPLE 7 Carbon black Vanb-lack HAP 3O Reflex blue in varnish No. 69884 3 Caladene 25 resin varnish in bodied linseed oil resin) 75 15%lead naphthenate (in hydrocarbon solvent) polarity stabiliser 50 Cold blend ingredients and mill.
Dilute then with 5 parts of Solvesso 100 to one part of paste by Weight.
The polarity of this toner is stable in Shell X55, Shell X4, n-hexane, n-heptane, Freon 11, Freon 113, and cyclohexane.
The following are descriptions of materials which have been referred to under their trademarks or registered trademarks.
Carbon black ISAF, particle size 23 millimicrons, manufactured by Australian Carbon Black Pty. Ltd.
Carbon black SRF, particle size '80 millimicrons, manufactured by Australian Carbon Black Pty. Ltd.
Carbon black Sterling MT, manufactured by Cabot C0.,
Carbon black Vanblack HAF, manufactured by R. T.
Vanderbilt C0., U.S.
Reflex blue in varnish No. 69 884, tinting ink for black,
manufactured by Reichhold Chemical.
Rhodene M8/50, short linseed oil alkyd, manufactured by Polymer Corp, Australia.
Dyal XOR 36, modified ether resin, manufactured by Sherwin-Williams Co.
Pentacite P-423, pentaerythritol resin, manufactured by Reichhold Chemical.
Superbeckacite 2100, oil reactive phenolic resin, manufactured by Reichhold Chemical.
Caladene 25, cresylic resin, manufactured by Polymer Corp., Australia.
Solvesso 100, hydrocarbon solvent, boiling range 160- 174 C., KB value 93, Standard Oil Co.
6 Shell X4petroleum fraction, boiling range 5846 C.,
KB value 30.
Shell X-petroleum fraction, boiling range 5 8-l40 C.,
KB value 40.
Freon ll-dichloromonofluoromethane, manufactured by Du Pont.
Freon l13trichlorotrifiuoroethane, manufactured by Du Pont.
What I claim is:
1. A liquid developer for electrostatic images consisting essentially of an electrically insulating carrier liquid of volume resistivity in excess of 1 0 ohm centimeter and a dielectric constant less than 3, particles of carbon black suspended in said carrier liquid as a toner, said carbon black particles having been previously wetted by grinding in an oil-containing dispersing medium, and a metallic soap in contact with said suspended particles of carbon black as a polarity stabilizer imparting positive polarity to such particles at least in the presence of a negative electrostatic field, said metallic soap being present in such quantity that the metal content of the soap is at least one percent by Weight of the carbon black particles in suspension, and said metallic soap being selected from the group consisting of the linoleates of the metals cobalt, manganese, lead and zinc, naphthenates and resinates of the metals calcium, cobalt, manganese, lead and zinc, octoates and oleates of the metals calcium and cobalt, palrnitate of the metal zinc and steanates of the metals aluminum, calcium, lead and zinc.
2. A liquid developer for electrostatic images in accordance with claim 1 wherein the linoleates, naphthenates, palmitate, stearates and resinates are present in such quantity that the metal content is not less than 1% and not greater than 25% by weight of the carbon black particles in suspension.
3. A liquid developer for electrostatic images in accordance with claim 1 wherein the octoates and oleates are present in such quantity that the metal content is not less than 1% and not greater than 2% by weight of the carbon black particles in suspension.
References Cited by the Examiner UNITED STATES PATENTS 2,907,674 10/1959 Metcalfe et al. 117 37 3,038,799 6/1962 Metcalfe et al. 9s 1 3,079,253 2/1963 Greig 117 17.s
JULIUS GREENWALD, Primary Examiner. V K. W. VERNON, J. D. WELSH, Assistant Examiners.
Claims (1)
1. A LIQUID DEVELOPER FOR ELECTROSTATIC IMAGES CONSISTING ESSENTIALLY OF AN ELECTRICALLY INSULATING CARRIER LIQUID OF VOLUME RESISTIVITY IN EXCESS OF 10**10 OHM CENTIMETER AND A DIELECTRIC CONSTANT LESS THAN 3, PARTICLES OF CARBON BLACK SUSPENDED IN SAID CARRIER LIQUID AS A TONER, SAID CARBON BLACK PARTICLES HAVING BEEN PREVIOUSLY WETTED BY GRINDING IN AN OIL-CONTAINING DISPERSING MEDIUM, AND A METALLIC SOAP IN CONTACT WITH SAID SUSPENDED PARTICLES OF CARBON BLACK AS A POLARITY STABILIZER IMPARTING POSITIVE POLARITY TO SUCH PARTICLES AT LEAST IN THE PRESENCE OF A NEGATIVE ELECTROSTATIC FIELD, SAID METALLIC SOAP BEING PRESENT IN SUCH QUANTITY THAT THE METAL CONTENT OF THE SOAP IS AT LEAST ONE PERCENT BY WEIGHT OF THE CARBON BLACK PARTICLES IN SUSPENSION, AND SAID METALLIC SOAP BEING SELECTED FROM THE GROUP CONSISTING OF THE LINOLEATES OF THE METALS COBALT, MANGANESE, LEAD AND ZINC, NAPHTHENATES AND RESINATES OF THE METALS CALCIUM, COBALT, MANGANESE, LEAD AND ZINC, OCTOATES AND OLEATES OF THE METALS CALCIUM AND COBALT, PALMITATE OF THE METAL ZINC AND STEARATES OF THE METALS ALUMINUM, CALCIUM, LEAD AND ZINC.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU11667/61A AU269029B2 (en) | 1961-11-23 | Improved liquid developer for electrostatic images |
Publications (1)
Publication Number | Publication Date |
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US3259581A true US3259581A (en) | 1966-07-05 |
Family
ID=3702349
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US237294A Expired - Lifetime US3259581A (en) | 1961-11-23 | 1962-11-13 | Liquid developer for electrostatic images |
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US (1) | US3259581A (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3411937A (en) * | 1965-03-01 | 1968-11-19 | Interchem Corp | Method of liquid electrostatic developing |
US3411936A (en) * | 1965-03-01 | 1968-11-19 | Interchem Corp | Developing electrostatic images with a liquid developer containing tetraphenyl tin or zirconyl 2-ethylhexoate |
US3438904A (en) * | 1966-01-10 | 1969-04-15 | Scm Corp | Liquid toner |
US3498917A (en) * | 1965-10-23 | 1970-03-03 | Philips Corp | Liquid developer for electrostatic images |
US3622368A (en) * | 1967-08-22 | 1971-11-23 | Ricoh Kk | Method for developing electrostatic latent images by utilizing coupling reaction |
US3850829A (en) * | 1972-07-05 | 1974-11-26 | Savin Business Machines Corp | Developing liquid for electrostatic images |
US3869397A (en) * | 1972-11-01 | 1975-03-04 | Gaf Corp | Electrostatic toner composition |
JPS511980B1 (en) * | 1968-08-19 | 1976-01-22 | ||
US3993483A (en) * | 1974-01-22 | 1976-11-23 | Canon Kabushiki Kaisha | Liquid developer for electrostatic image |
US4093534A (en) * | 1974-02-12 | 1978-06-06 | Plessey Handel Und Investments Ag | Working fluids for electrophoretic image display devices |
US4155862A (en) * | 1975-06-25 | 1979-05-22 | Konishiroku Photo Ind. Co., Ltd. | Liquid developer for color electrophotography and process for preparation of the same |
US4740444A (en) * | 1986-04-30 | 1988-04-26 | E. I. Du Pont De Nemours And Company | Process for preparation of electrostatic liquid developing using metallic soap as adjuvant |
US4820605A (en) * | 1987-11-25 | 1989-04-11 | E. I. Du Pont De Nemours And Company | Modified liquid electrostatic developer having improved image scratch resistance |
US5407771A (en) * | 1984-12-10 | 1995-04-18 | Indigo N.V. | Toner and liquid composition using same |
US20060194138A1 (en) * | 2005-02-28 | 2006-08-31 | Keren Regev | Liquid toner methods of producing same |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US907674A (en) * | 1907-09-28 | 1908-12-22 | Hobbs Mfg Company | Scoring-machine. |
US3038799A (en) * | 1958-01-13 | 1962-06-12 | Commw Of Australia | Method of reversing the image in xerography |
US3079253A (en) * | 1957-06-19 | 1963-02-26 | Rca Corp | Method of electrophotography employing a heat glossing composition |
-
1962
- 1962-11-13 US US237294A patent/US3259581A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US907674A (en) * | 1907-09-28 | 1908-12-22 | Hobbs Mfg Company | Scoring-machine. |
US3079253A (en) * | 1957-06-19 | 1963-02-26 | Rca Corp | Method of electrophotography employing a heat glossing composition |
US3038799A (en) * | 1958-01-13 | 1962-06-12 | Commw Of Australia | Method of reversing the image in xerography |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3411937A (en) * | 1965-03-01 | 1968-11-19 | Interchem Corp | Method of liquid electrostatic developing |
US3411936A (en) * | 1965-03-01 | 1968-11-19 | Interchem Corp | Developing electrostatic images with a liquid developer containing tetraphenyl tin or zirconyl 2-ethylhexoate |
US3498917A (en) * | 1965-10-23 | 1970-03-03 | Philips Corp | Liquid developer for electrostatic images |
US3438904A (en) * | 1966-01-10 | 1969-04-15 | Scm Corp | Liquid toner |
US3622368A (en) * | 1967-08-22 | 1971-11-23 | Ricoh Kk | Method for developing electrostatic latent images by utilizing coupling reaction |
JPS511980B1 (en) * | 1968-08-19 | 1976-01-22 | ||
US3850829A (en) * | 1972-07-05 | 1974-11-26 | Savin Business Machines Corp | Developing liquid for electrostatic images |
US3869397A (en) * | 1972-11-01 | 1975-03-04 | Gaf Corp | Electrostatic toner composition |
US3993483A (en) * | 1974-01-22 | 1976-11-23 | Canon Kabushiki Kaisha | Liquid developer for electrostatic image |
US4093534A (en) * | 1974-02-12 | 1978-06-06 | Plessey Handel Und Investments Ag | Working fluids for electrophoretic image display devices |
US4155862A (en) * | 1975-06-25 | 1979-05-22 | Konishiroku Photo Ind. Co., Ltd. | Liquid developer for color electrophotography and process for preparation of the same |
US5407771A (en) * | 1984-12-10 | 1995-04-18 | Indigo N.V. | Toner and liquid composition using same |
US4740444A (en) * | 1986-04-30 | 1988-04-26 | E. I. Du Pont De Nemours And Company | Process for preparation of electrostatic liquid developing using metallic soap as adjuvant |
US4820605A (en) * | 1987-11-25 | 1989-04-11 | E. I. Du Pont De Nemours And Company | Modified liquid electrostatic developer having improved image scratch resistance |
US20060194138A1 (en) * | 2005-02-28 | 2006-08-31 | Keren Regev | Liquid toner methods of producing same |
US7736828B2 (en) * | 2005-02-28 | 2010-06-15 | Hewlett-Packard Development Company, L.P. | Liquid toner methods of producing same |
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